HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 135543774, compound → HCID 136384193, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 135543774 | HCID 135543774 | — |
| Reactant | HCID 136388582 | HCID 136388582 | — |
| Product | HCID 136384193 | HCID 136384193 | 100% |
Reaction Steps
Using a method similar to Example (S)-8-fluoro-2-trifluoromethyl-11-[3-(2-methoxy-ethyl)-4-methyl-piperazin-1-yl]-5H-dibenzo[b,e][1,4]diazepine succinate, using (S)-8-chloro-2-trifluoromethyl-11-[3-(2-methoxy-ethyl)-piperazin-1-yl]-5H-dibenzo[b,e][1,4]diazepine (0.051 g, 0.12 mmol) to give 0.054 g (100% yield) of the free base as a yellow oil which is converted to the succinate salt as described previously: Mass Spectrum (m/e): 454(M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07384934B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-7de3ff5d77e94d15bee512ec1bcb5dd1 |
| Source note | uspto-grants-2008_06 |